The DBAF has been a life saver for us! They’ve supplied us with the knowledge and the resources to fight off anything DBA might throw at us.
Amelia – 8 years
Drew – 2 years
Good things come in small packages! I may be little, but I’m a fighter – DBA… no contest.
David – 1 month(now 12 years)
This is David at 1 month old weighing almost 2 pounds. DBA changed our paths in life, but I will ALWAYS be there to hold his hand for he holds my heart.
Emmalynn – 3 years
Living with DBA has had its ups and downs, but with all the love and support we have gotten from our family and friends, we have been able to provide our daughter with the best life possible.
YouKai (Stephen) – 5 years
We are hopeful that a cure will be discovered soon so that our son doesn’t have to endure pokes and disruptions and can feel good all the time – isn’t that what every child deserves?
Lydia – 6 years
James Thomas – 3 years
Never give up on something that you can’t go a day without thinking about.
Nathaniel – 7 years
With something so rare, our biggest fear was that our son would battle DBA alone, he never does. Thank you DBA Foundation!
Corey & Tessa Ann – 27 years & 10 months
Living everyday to fight DBA
Jensen – 4 years
Living with DBA is challenging and confusing at times but with the DBAF by your side their information and guidance is PRICELESS.